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Merck
CN

48076

Carbazole solution

certified reference material, 2000 μg/mL in methylene chloride

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About This Item

CAS Number:
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

SMILES string

c1ccc2c(c1)[nH]c3ccccc23

InChI key

UJOBWOGCFQCDNV-UHFFFAOYSA-N

grade

certified reference material, TraceCERT®

packaging

ampule of 1 mL

concentration

2000 μg/mL in methylene chloride

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

Quality Level

General description

Carbazole is a cheap kind of raw material, obtained from the distillation process of coal tar, which can be used to prepare carbazole based polymers, which can find a broad array of applications in electrophotographic materials, photorefractive materials and photovoltaic devices.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

危险化学品
This item has

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Carbazole-containing polymers: synthesis, properties and applications
Grazulevicius.V.J, et al.
Progress in Polymer Science, 28, 1297-1353 (2003)
Cui Zhao et al.
Environmental science & technology, 46(11), 6205-6213 (2012-05-15)
This study aims to establish a systematic method to optimize the bacterial consortium for the simultaneous biodegradation of multixenobiotics in wastewater. Three nitrogen heterocyclic compounds (NHCs), pyridine, quinoline, and carbazole, were chosen as the target compounds with each about 200
Isis E Mejías Carpio et al.
Nanoscale, 4(15), 4746-4756 (2012-07-04)
It is critical to develop highly effective antimicrobial agents that are not harmful to humans and do not present adverse effects on the environment. Although antimicrobial studies of graphene-based nanomaterials are still quite limited, some researchers have paid particular attention
Shen H Tan et al.
Organic letters, 14(22), 5621-5623 (2012-10-31)
The racemic modification of the Aspidosperma alkaloid limaspermidine (1) has been prepared in ten steps including one involving a Raney-cobalt-mediated tandem reductive cyclization of nitrile 8 to give the tetracyclic system 9b. Compound (±)-1 has been converted over two steps
Yagang Chen et al.
Macromolecular rapid communications, 33(20), 1759-1764 (2012-07-06)
Two conjugated polymers (CPs) P-tCzC12 and P-tCzC16 comprising alternating dithieno[3,2-b:6,7-b]carbazole and 4,4'-dihexadecyl-2,2'-bithiophene units have been designed and synthesized. Upon thermal annealing, they can form ordered thin films in which the polymer backbones dominantly adopted an edge-on orientation respective to the

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